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Effectiveness of Viscum Album Mother Tincture as an Anti-hypertensive in Essential Hypertension

Effectiveness of Viscum Album Mother Tincture as an Anti-hypertensive in Essential Hypertension. One Group Pretest Posttest Design

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01527760
Enrollment
37
Registered
2012-02-07
Start date
2011-02-28
Completion date
2011-09-30
Last updated
2012-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Essential Hypertension, Viscum album mother tincture, one group pretest post-test study

Brief summary

To estimate the effectiveness of Viscum album Homoeopathic mother tincture in Essential Hypertension by conducting clinical trial in moderate hypertensive patients for a period of six weeks.

Interventions

DRUGViscum album ethanolic extract manufactured according to Homoeopathic pharmacopoeia of India (H.P.I.)

Ten drops of Drug in 30 ml of distilled water with a frequency of three times a day for a duration of 12 weeks

Sponsors

Rajiv Gandhi University of Health Sciences
CollaboratorOTHER
Fr Muller Homoeopathic Medical College
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hypertension at the range 180-120 mm of Hg for Systole & * 110-80 mm of Hg for Diastole

Exclusion criteria

* Patients who are on ACEI / ARB for Hypertension * Diseases in which life expectancy is less than six months * Secondary hypertension * CHD * Family History of Mental Illness like Anxiety or depression. * Nasal Congestion

Design outcomes

Primary

MeasureTime frame
Change in Systolic and Diastolic blood pressure.12 weeks

Secondary

MeasureTime frameDescription
Change in Serum Cholesterol12 weeks
Change in Serum Triglycerides12 weeks
Change in Serum LDH12 weeks
Change in Serum Urea12 weeks
change in Serum CKMB12 weeks and 16 weeksThe blood sample was collected at the end of 12 weeks of medication followed by a drug free period of 4 weeks.The blood sample was collected again at the end of 4 weeks of drug free period to ascertain serum CKMB.

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026